An azoospermic male with a novel chromosome 46, XX, der(15)t(Y; 15)(p11.3; p12).

Jiebin Wu, Guanli Hu, Jingfang Zhai, Conghui Han, Zhenbei Li

Abstract readCase Reports

In one paragraph

Article in Clinical case reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in

1citing papers in PubMed

–field-weighted citation impact

1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

An azoospermic male with a novel chromosome 46, XX, der(15)t(Y; 15)(p11.3; p12).Clinical case reports · 2022
Article

4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Jiebin WuDepartment of Prenatal Diagnosis Medical Center Xuzhou Central Hospital, Xuzhou Clinical Schools of Nanjing Medical University and Xuzhou Medical University Xuzhou Jiangsu China.

Guanli HuDepartment of Prenatal Diagnosis Medical Center Xuzhou Central Hospital, Xuzhou Clinical Schools of Nanjing Medical University and Xuzhou Medical University Xuzhou Jiangsu China.

Jingfang ZhaiDepartment of Prenatal Diagnosis Medical Center Xuzhou Central Hospital, Xuzhou Clinical Schools of Nanjing Medical University and Xuzhou Medical University Xuzhou Jiangsu China.ORCID https://orcid.org/0000-0001-7109-3193

Conghui HanDepartment of Urology Xuzhou Central Hospital, Xuzhou Clinical Schools of Nanjing Medical University and Xuzhou Medical University Xuzhou Jiangsu China.

Zhenbei LiDepartment of Urology Xuzhou Central Hospital, Xuzhou Clinical Schools of Nanjing Medical University and Xuzhou Medical University Xuzhou Jiangsu China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Male individuals with a 46, XX karyotype are commonly diagnosed with 46, XX male sex reversal syndrome, one of the rarest sex chromosomal anomalies. In this case, we report a rare XX male with Y-specific DNA sequences located near the end of chromosome 15 p-arm, which was verified by fluorescent in situ hybridization (FISH) as well as copy number variation sequencing (CNV-seq) based on the next- generation sequencing method (>100 Kb). To the best of our knowledge, there have been no reports of XX male with the Yp region transferred to the terminal of chromosome 15 short arm.

Indexed as

46, XX maleazoospermiacytogeneticsmolecular geneticspositive SRY gene

Identifiers

PMID35846903

DOI10.1002/ccr3.5984

PMCPMC9272210

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.